Judith Knops

784 total citations
12 papers, 388 citations indexed

About

Judith Knops is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Judith Knops has authored 12 papers receiving a total of 388 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Judith Knops's work include Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Ion channel regulation and function (2 papers). Judith Knops is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Prenatal Screening and Diagnostics (3 papers) and Ion channel regulation and function (2 papers). Judith Knops collaborates with scholars based in United States, France and Poland. Judith Knops's co-authors include Tatsuo Yamamoto, Sue Ann Berend, Kazuso Iinuma, Masaji Nagaishi, Richard Jensen, Alfred L. George, George Bosworth Brown, Brian A. Van Tine, Jianying Han and W H Finley and has published in prestigious journals such as Journal of Virology, American Journal of Obstetrics and Gynecology and Genomics.

In The Last Decade

Judith Knops

12 papers receiving 368 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Judith Knops United States 9 219 103 93 88 85 12 388
Jorge M. Tolosa Australia 9 219 1.0× 73 0.7× 84 0.9× 33 0.4× 11 0.1× 19 520
Jean‐Marie Rival France 12 191 0.9× 17 0.2× 72 0.8× 186 2.1× 29 0.3× 24 370
Rosemarie Rupps Canada 12 153 0.7× 29 0.3× 60 0.6× 122 1.4× 27 0.3× 23 337
Abeltje M. Polstra Netherlands 12 204 0.9× 108 1.0× 118 1.3× 256 2.9× 10 0.1× 18 523
Shulamit Metzger Israel 7 211 1.0× 44 0.4× 10 0.1× 66 0.8× 150 1.8× 8 463
Phillip L. Van United States 7 170 0.8× 53 0.5× 18 0.2× 309 3.5× 109 1.3× 7 487
S. M. Khorshed Alam United States 13 195 0.9× 39 0.4× 120 1.3× 86 1.0× 15 0.2× 21 572
Francisco Galán Spain 12 106 0.5× 16 0.2× 63 0.7× 139 1.6× 15 0.2× 18 355
Meenakshi Bhat India 10 171 0.8× 64 0.6× 24 0.3× 115 1.3× 18 0.2× 32 370
Heidi Gildersleeve United States 7 400 1.8× 20 0.2× 27 0.3× 176 2.0× 44 0.5× 8 667

Countries citing papers authored by Judith Knops

Since Specialization
Citations

This map shows the geographic impact of Judith Knops's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Judith Knops with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Judith Knops more than expected).

Fields of papers citing papers by Judith Knops

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith Knops. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Judith Knops. The network helps show where Judith Knops may publish in the future.

Co-authorship network of co-authors of Judith Knops

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Knops. A scholar is included among the top collaborators of Judith Knops based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Judith Knops. Judith Knops is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Donnenfeld, Alan E., et al.. (2006). Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency. American Journal of Obstetrics and Gynecology. 194(2). 508–511. 16 indexed citations
2.
Nagaishi, Masaji, et al.. (2004). Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan. Journal of obstetrics and gynaecology research. 30(3). 237–241. 86 indexed citations
3.
Tine, Brian A. Van, John C. Kappes, N. Sanjib Banerjee, et al.. (2004). Clonal Selection for Transcriptionally Active Viral Oncogenes during Progression to Cancer. Journal of Virology. 78(20). 11172–11186. 98 indexed citations
4.
Knops, Judith, et al.. (2001). In situ analysis of the transcriptional activity of integrated viral DNA using tyramide-FISH.. PubMed. 106. 381–5. 15 indexed citations
5.
Tine, Brian A. Van, Judith Knops, George M. Shaw, & Win May. (1999). Assignment<footref rid="foot01"><sup>1</sup></footref> of human MFNG, manic fringe Drosophila homolog, to 22q13.1 using tyramide fluorescence in situ hybridization (T-FISH). Cytogenetic and Genome Research. 87(1-2). 132–133. 1 indexed citations
6.
Tine, Brian A. Van, Judith Knops, Adam P. Butler, et al.. (1998). Localization ofHuC(ELAVL3) to Chromosome 19p13.2 by Fluorescencein SituHybridization Utilizing a Novel Tyramide Labeling Technique. Genomics. 53(3). 296–299. 13 indexed citations
7.
Han, Jian, Judith Knops, John Longshore, & Peter H. King. (1996). Localization ofHuman elav-like Neuronal Protein 1(Hel-N1) on Chromosome 9p21 by Chromosome Microdissection Polymerase Chain Reaction and Fluorescencein SituHybridization. Genomics. 36(1). 189–191. 6 indexed citations
8.
Descartes, Maria, Kim M. Keppler‐Noreuil, Judith Knops, et al.. (1996). Terminal deletion of the long arm of chromosome 4 in a mother and two sons. Clinical Genetics. 50(6). 538–540. 26 indexed citations
9.
George, Alfred L., Harry A. Drabkin, Jianying Han, et al.. (1995). Assignment of the human heart tetrodotoxin-resistant voltage-gated Na<sup>+</sup> channel α-subunit gene (SCN5A) to band 3p21. Cytogenetic and Genome Research. 68(1-2). 67–70. 87 indexed citations
10.
George, Alfred L., et al.. (1994). Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23. Genomics. 19(2). 395–397. 9 indexed citations
11.
Takaesu, Norma T., et al.. (1992). Molecular and cytogenetic investigation of complex tissue‐specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype. American Journal of Medical Genetics. 43(3). 554–560. 7 indexed citations
12.
Knops, Judith & Richard Jensen. (1980). Morphological and Phenolic Variation in a Three Species Community of Red Oaks. Bulletin of the Torrey Botanical Club. 107(3). 418–418. 24 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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